Topical formulations comprising 1-N-arylpyrazole derivatives and amitraz

ABSTRACT

The present invention provides for, inter alia, novel topical formulations comprising at least one 1-N-arypyrazole derivative and amitraz and to methods for treating, controlling, or preventing parasite infestations on mammals or birds The inventive formulations include spot-on, pour-on or spray formulations and may include a further ectoparasiticide, such as an IGR compound, an avermectin or milbemycin derivative, or a pyrethroid insecticides, and anthelmintics, such as benzimidazoles and imidazothiazoles. The inventive formulation provides a larger duration of parasite control at a faster rate of control. The inventive formula remains effective up to three months from the first application. Moreover, the inventive formulations prevent tick attachment to the animal, thereby providing protection against tick borne diseases. The ectoparasites which may be controlled, treated or prevented by the present invention includes ticks, fleas, mites, mange, lice, mosquitoes, flies and cattle grubs.

RELATED APPLICATIONS

The application claim priority to provisional application U.S. Ser. No.60/530,525, filed Dec. 17, 2003, herein incorporated by reference.Reference is also made to application U.S. Ser. No. 10/374,627 filedFeb. 26, 2003, entitled 1-N-arylpyrazole Derivatives in Prevention ofArthropod-Borne and Mosquito-Borne Diseases. This application and allapplications and prior publications either therein or cited herein(including documents cited in the text or during prosecution) areexpressly incorporated by reference.

FIELD OF THE INVENTION

This invention provide for, inter alia, novel topical formulationscomprising at least one 1-N-arylpyrazole derivatives and amitraz and tomethods for treating parasite infestations in mammals and birds bytopically applying the inventive formulations to said mammals and birds.The inventive formulation exhibit activity against ectoparasites such asfleas and ticks, that is far superior than formulations comprising an1-N-arypyrazole derivative alone, such as fipronil, thereby indicatingsynergy. This result is even more surprising given the fact that amitrazis not recognized in the field as a flea product.

BACKGROUND OF THE INVENTION

Parasitic diseases may be caused by either endoparasites orectoparasites. As used herein endoparasites refer to those parasitesliving inside the body of the host, either within an organ (such as thestomach, lungs, heart, intestines, etc.) or simply under the skin.Ectoparasites are those parasites that live on the outer surface of thehost but still draw nutrients from the host. Endoparasitic diseases mayfurther be subdivided based on class of parasite involved in theinfection. For example, endoparasitic diseases generally referred to ashelminthiasis are due to infection of the host with parasitic wormsknown as helminths. Helminthiasis is a prevalent and serious worldwideeconomic problem involving infection of domesticated animals such asswine, sheep, horses, cattle, goats, dogs, cats, and poultry. Many ofthese infections, caused by the group of worms described as nematodes,cause diseases in various species of animals throughout the world. Thesediseases are frequently serious and can result in the death of theinfected animal. The most common genera of nematodes infecting theanimals referred to above include, but are not limited to, Haemonchus,Trichostrongylus, Ostertagia, Nematodirus, Cooperia, Ascaris,Bunostomum, Oesophagostomum, Chabertia, Trichuris, Strongylus,Trichonema, Dictyocaulus, Capillaria, Heterakis, Toxocara, Ascaridia,Oxyuris, Ancylostoma, Uncinaria, Toxascaris, and Parascaris. Manyparasites are species specific (infect only one host) and most also havea preferred site of infection within the animal. Thus, Haemonchus andOstertagia primarily infect the stomach while Nematodirus and Cooperiamostly attack the intestines. Other endoparasites reside in the heart,eyes, lungs, blood vessels, and the like while still others aresubcutaneous parasites. Helminthiasis can lead to weakness, weight loss,anemia, intestinal damage, malnutrition, and damage to other organs. Ifleft untreated these diseases can result in the death of the animal.

Examples of endoparasites which infect animal and man include but arenot limited to gastro-intestinal parasites of the genera Ancylostoma,Necator, Ascaris, Strongyloides, Trichinella, Capillaria, Trichuris,Enterobius, and the like. Other endoparasites which infect animal andman are found in the blood or in other organs. Examples of suchparasites include but are not limited to filarial worms Wuchereria,Brugia, Onchocerca, and the like as well as extra-intestinal stages ofthe intestinal worms Strongylides and Trichinella. Ectoparasites whichinfest man and domestic animals include arthropods, such as ticks,fleas, mites, mosquitos, lice, and the like and infections by theseparasites can result in transmission of serious and even fatal diseases.

Infestations by ectoparasitic arthropods including but not limited toticks, mites, lice, stable flies, hornflies, blowflies, face flies,fleas, mosquitoes and the like are also a serious problem. Infection bythese parasites results not only in loss of blood and skin lesions, butalso can interfere with normal eating habits thus causing weight loss.Ectoparasitic infestations of a host can also result in transmission ofserious diseases including but not limited to encephalitis,anaplasmosis, babesiosis, rocky mountain spotted fever, lyme disease,ehrlichiosis, West Nile virus, swine pox, malaria, yellow fever, and thelike, many of which can be fatal to the host. Animals may be infected byseveral species of parasite at the same time since infection by oneparasite may weaken the animal and make it more susceptible to infectionby a second species of parasite.

Many of the compounds used in this invention are also active againsthousehold pests including but not limited to cockroach, Blatella sp.,clothes moth, Tineola sp., carpet beetle, Attagenus sp. and the houseflyMusca domestica and against Solenopsis invicta (imported fire ants),termites, and the like.

These compounds are furthermore useful against agricultural pests suchas aphids (Acyrthiosiphon sp.) locusts, and boll weevils as well asagainst insect pest which attack stored grains such as Tribolium sp. andagainst immature stages of insects living on plant tissue. The compoundsare also useful as a nematodicide for the control of soil nematodes,which may be agriculturally important.

Antiparasitic agents are also useful for the treatment and/or preventionof helminthiasis in domestic animals such as cattle, sheep, horses,dogs, cats, goats, swine, and poultry. They are also useful in theprevention and treatment of parasitic infections of these animals byectoparasites such as ticks, mites, lice, fleas, mosquitoes and thelike. They are also effective in the treatment of parasitic infectionsof humans.

Various methods of formulating antiparasitical formulations are known inthe art. These include oral formulations, baits, dietary supplements,powders, shampoos, etc. Formulations for localized topical applicationsof antiparasitical formulations are also known in the art. For example,pour-on solutions comprising 1-N-phenylpyrazole derivatives, such asfipronil, are known in the art and are described in, for example, U.S.Pat. No. 6,010,710, U.S. Pat. No. 6,413,542, U.S. Pat. No. 6,001,384,U.S. Pat. No. 6,413,542 as well as copending application Ser. No.10/120,691, filed Apr. 11, 2002 and now allowed. Other methods offormulating antiparasitic agents include spot-on formulations or spays.

Spot-on formulations are well known techniques for topically deliveringan antiparasitic agent to a limited area of the host. For example, U.S.Pat. No. 5,045,536 describes such formulations for ectoparasites. Otherspot-on formulations include U.S. Pat. No. 6,426,333 and U.S. Pat. No.6,482,425 and application U.S. Ser. No. 10/155,397, now allowed andpublished as Publication No. U.S. 2003-0050327A1. Reference is also madeto Publication No. U.S. 2003-166688A1. WO 01/957715 describes a methodfor controlling ectoparasites in small rodents as well as interruptingor preventing the diseases caused by arthropods or small rodents, whichcomprise applying topical formulations, such as spot-on compositions, tothe skin, or hair of the rodents.

1-N-arylpyrazoles as a class of chemicals are well known in the art, aswell as methods for their use in controlling parasites includinginsects, such as fleas, ticks, lice or mosquitoes in mammals, such asdomesticated livestock or companion animals or birds, either alone or incombination with other pesticides such as insect growth regulators. See,e.g., EP-A-295,217, EP 295 177, EP-A-840-686, EP-A-352,944, WO 00/35844,WO 98/39972, U.S. Pat. Nos. 5,122,530 5,236,938, 5,232,940, 5,576,4295,814,652, 5,567,429, 6,090,751 and 6,096,329 as well as Publication No.US 2002-90381-A1. See also copending applications U.S. Ser. Nos.07/719,942; 08/933,016; 09/174,598; 08/863,182; and 08/863,692. Thecompounds of the families defined in these patents are extremely activeand one of these compounds,5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinylpyrazole,or fipronil, is particularly effective, but not exclusively effective,against fleas and ticks. The 1-arylpyrazoles exert their activity bybeing distributed through the sebaceous glands of the animal.

WO-A-87/3781, EP-A-295,117 and EP-A-500,209 describe a class ofinsecticides which are N-phenyl-pyrazole derivatives. These compoundsare given as having activity against a very large number of parasites,including Boophilus microplus, fleas, ticks and lice in fields as variedas agriculture, public health and veterinary medicine. The generalteaching of these documents indicates that these insecticidal compoundsmay be administered via different routes: oral, parenteral, percutaneousand topical routes. Topical administration comprises, in particular,oral formulations, baits, dietary supplements, skin solutions (pour-onor spot-on), sprays, drenches, baths, showers, jets, powders, greases,shampoos, creams, etc. The pour-on type skin solutions are designed forpercutaneous administration. Example 9 of EP-A-295,117 and Example 29Iof EP-A-500,209 describe a pour-on type skin solution containing 15%insecticide and 85% dimethyl sulphoxide, for percutaneous administrationof the insecticide. 1-N-arylpyrazole derivatives are known in the art toprevent, treat or control ectoparasite infestation in mammals, such ascats, dogs and cattle.

Amitraz is known in the art as a pesticide and is used to control redspider mites, leaf mites, scale insects and aphids. In animals, amitrazis used to control tick, mites, and lice. Extoxnethttp://ace.orst.edu/info/extonet/pips/amitraz.html. However, amitraz isnot known in the art to treat fleas Amitraz belongs to the amidinechemical family and has the following structure:

Amitraz is described in U.S. Pat. No. 3,781,355 and U.S. Pat. No.3,864,497.

Other compounds that are known in the art to present, treat or controlendo- and ectoparasite infestation include milbemycin or avermectinderivatives. The avermectin and milbemycin series of compounds arepotent anthelmintic and antiparasitic agents against a wide range ofinternal and external parasites. The compounds which belong to thisseries are either natural products or are semi-synthetic derivativesthereof. The structures of these two series of compounds are closelyrelated and they both share a complex 16-membered macrocyclic lactonering; however, the milbemycin do not contain the aglycone substituent inthe 13-position of the lactone ring. The natural product avermectins aredisclosed in U.S. Pat. No. 4,310,519 to Albers-Schonberg, et al., andthe 22, 23-dihydro avermectin compounds are disclosed in Chabala, etal., U.S. Pat. No. 4,199,569. For a general discussion of avermectins,which include a discussion of their uses in humans and animals, see“Ivermectin and Abamectin,” W. C. Campbell, ed., Springer-Verlag, NewYork (1989). Naturally occurring milbemycins are described in Aoki etal., U.S. Pat. No. 3,950,360 as well as in the various references citedin “The Merck Index” 12^(th) ed., S. Budavari, Ed., Merck & Co., Inc.Whitehouse Station, N.J. (1996). Semisynthetic derivatives of theseclasses of compounds are well known in the art and are described, forexample, in U.S. Pat. No. 5,077,308, U.S. Pat. No. 4,859,657, U.S. Pat.No. 4,963,582, U.S. Pat. No. 4,855,317, U.S. Pat. No. 4,871,719, U.S.Pat. No. 4,874,749, U.S. Pat. No. 4,427,663, U.S. Pat. No. 4,310,519,U.S. Pat. No. 4,199,569, U.S. Pat. No. 5,055,596, U.S. Pat. No.4,973,711, U.S. Pat. No. 4,978,677, and U.S. Pat. No. 4,920,148.

Avermectins and milbemycins share the same common 16-memberedmacrocyclic lactone ring; however, milbemycins do not possess thedisaccharide substituent on the 13-position of the lactone ring. Whilemany avermectin compounds are known in the art, a representativestructure of the class of compounds is as follows:

where the broken line indicates a single bond at the 22,23-positions;

-   -   R₁ is hydrogen or hydroxy provided that R₁ is present only when        the broken line indicates a single bond;    -   R₂ is alkyl of from 1 to 6 carbon atoms or alkenyl of from 3 to        6 carbon atoms or cycloalkyl of from 3 to 8 carbon atoms;    -   R₃ is hydroxy, methoxy or ═NOR₅ where R₅ is hydrogen or lower        alkyl; and    -   R₄ is hydrogen, hydroxy or

-   -   where R₆ is hydroxy, amino, mono- or di-lower alkylamino or        lower alkanoylamino.

The preferred compounds are avermectin Bla/Blb (abamectin),22,23-dihydro avermectin Bla/Blb (ivermectin) and the4″-acetylamino-5-ketoximino derivative of avermectin Bla/Blb. Bothabamectin and ivermectin are approved as broad spectrum antiparasiticagents.

The structures of abamectin and ivermectin are as follows:

-   -   wherein for abamectin the broken line represents a double bond        and R₁ is not present and for ivermectin the double bond        represents a single bond and R₁ is hydrogen; and

R₂ is isopropyl or sec-butyl.

The 4″-acetyl amino-5-ketoximino derivatives of avermectin Bla/Blb hasthe following structural formula:

where R₂ is isopropyl or sec-butyl.

The avermectin products are generally prepared as a mixture of at least80% of the compound where R₂ is sec-butyl and no more than 20% of thecompound where R₂ is isopropyl.

Other preferred avermectins, include emamectin, eprinomectin anddoramectin. Doramectin is disclosed in U.S. Pat. No. 5,089,490 and EP214 738. This compound has the following structure:

In the present formulations, ivermectin and eprinomectin are especiallypreferred.

A representative structure for a milbemycin is that for milbemycin α₁:

An especially preferred avermectin is moxidectin, whose structure is asfollows:

The compound is disclosed in U.S. Pat. No. 5,089,490.

Other classes of compound are known to treat endo-and ectoparasites.These classes include benzimidazoles, which are effective againsttapeworms, lungworms and roundworms, imidazothiazoles, which areeffective against roundworms, tapeworms and lungworms, and thepyrethroids. Examples of benzimidazoles inclcude albendazole (U.S. Pat.No. 3,915,986); fenbenzazole (U.S. Pat. No. 3,954,791), mebendazole(U.S. Pat. No. 3,657,261), oxibenzazole (U.S. Pat. No. 3,574,845) andtriclabenzazole (U.S. Pat. No. 4,197,307). An example of animidazothiazole is levamisole (U.S. Pat. No. 3,529,350).

The pyrethoids are a class of naturally occurring or syntheticallyderived insecticide. Their compounds are particularly effective againstWest Nile virus. Synthetic pyrethroids include pyrethrin I and pyrethrinII. Synthetic pyrethroids include permethrin (U.S. Pat. No. 4,113,968),resmethrin, and sumithrin (U.S. Pat. Nos. 3,934,023 and 2,348,930).

SUMMARY OF THE INVENTION

The present invention provides for, inter alia, novel topicalformulations comprising at least one 1-N-arypyrazole derivative andamitraz and to methods for treating, controlling, or preventing parasiteinfestations on mammals or birds The inventive formulations includespot-on, pour-on or spray formulations and may include a furtherectoparasiticide, such as an IGR compound, an avermectin or milbemycinderivative, or a pyrethroid insecticides, and anthelmintics, such asbenzimidazoles and imidazothiazoles. The inventive formulation providesa larger duration of parasite control at a faster rate of control. Theinventive formula remains effective up to three months from the firstapplication. Moreover, the inventive formulations prevent tickattachment to the animal, thereby providing protection against tickborne diseases. The ectoparasites which may be controlled, treated orprevented by the present invention includes ticks, fleas, mites, mange,lice, mosquitoes, flies and cattle grubs.

More specifically, the present invention provides for, inter alia, aparasitical spot-on formulation, which comprises:

-   -   a) an effective amount of an ectoparasitical combination        comprising an 1-N-arylpyrazole derivative and amitraz;    -   b) a pharmaceutical or veterinary acceptable liquid carrier        vehicle;    -   c) optionally, a crystallization inhibitor.        This invention further provides for a parasitical pour-on        formulation, which comprises:    -   a) an effective amount of an ectoparasitical combination        comprising an 1-N-arylpyrazole derivative and amitraz;    -   b) a pharmaceutical or veterinary acceptable liquid carrier        vehicle;    -   c) optionally, a crystallization inhibitor; and    -   d) optionally, an antioxidant.        Also provided for in the present invention is a parasitical        spray formulation, which comprises:    -   a) an effective amount of an ectoparasitical combination        comprising an 1-N-arylpyrazole derivative and amitraz;    -   b) a pharmaceutical or veterinary acceptable liquid carrier        vehicle.

A further embodiment of the present invention are spot-on, pour-on orspray formulations that further comprise at least one additionalantiparasiticidal or anthelmintic agent, such as an IGR compound, amilbemycin or avermectin derivative, a pyrethroid, a benzimidazole, suchas albendazole, fenbenzazole, mebendazole, oxibendazole, ortriclobendazole, or a imidazothiazole, such as levamisole.

The present invention further provides for a method for preventing,eliminating or controlling parasites in a mammal or bird in need thereofor an environment where they reside, which comprises applying aneffective amount of the inventive spot-on, pour-on or spray formulationto the mammal or bird. Animals include mammals, such as dog, cats,zebras and horses, and birds, such as chickens, turkeys and quail.Environments include animal houses, such as dog or cat bedding, horsestables and chicken litter.

DETAILED DESCRIPTION OF THE INVENTION

Other objects, features and aspects of the present invention aredisclosed in, or are obvious from, the following Detailed Description.It is to be understood by one of ordinary skill in the art that thepresent discussion is a description of exemplary embodiments only and isnot intended as limiting the broader aspects of the present invention,which broader aspects are embodied in the exemplary construction. Infact, it will be apparent to those skilled in the art that variousmodifications and variations can be made in the present inventionwithout departing from the scope or spirit of the invention. Forinstance, features illustrated or described as part of one embodimentcan be used in another embodiment to yield a still further embodiment.It is intended that the present invention cover such modifications andvariations as come within the scope of the appended claims and theirequivalents.

For convenience, certain terms employed in the Specification, Examples,and appended claims are collected here.

Definitions: As used herein, the term “comprising” in this disclosurecan mean “including” or can have the meaning commonly given to the term“comprising” in U.S. Patent Law.

Preferred topical formulations include those formulations wherein the1-arylpyrazol is a compound of the formula:

-   -   in which:    -   R₁ is a halogen atom, CN or alkyl;    -   R₂ is S(O)_(n)R₃ or 4,5-dicyanoimidazol-2-yl or haloalkyl;    -   R₃ is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl or        haloalkyl;    -   R₄ is hydrogen, halogen, NR₅R₆, S(O)_(m)R₇, C(O)R₇, C(O)OR₇,        alkyl, haloalkyl, OR₈ or —N═C(R₉)(R₁₀) substituent;    -   R₅ and R₆ independently represent a hydrogen atom, alkyl,        haloalkyl, C(O)alkyl, S(O)_(r)CF₃ or alkoxycarbonyl or R₅ and R₆        together may combine to form a ring of 5 to 7 members.    -   R₇ represents an alkyl or haloalkyl group;    -   R₈ represents an alkyl, haloalkyl or a hydrogen;    -   R₉ represents an alkyl or a hydrogen;    -   R₁₀ represents an optionally substituted aryl or an optionally        substituted heteroaryl group;    -   R₁₁ and R₁₂ represent, independently of one another, hydrogen,        halogen CN or NO₂;    -   R₁₃ represents a halogen atom or a haloalkyl, haloalkoxy,        S(O)_(q)CF₃ or SF₅ group;    -   m, n, q and r represent, independently of one another, an        integer equal to 0, 1 or 2;    -   X represents a trivalent nitrogen atom or a C—R₁₂, the three        other valencies of the carbon atom forming part of the aromatic        ring optionally with a pharmaceutically acceptable carrier or        excipient.

A more preferred formulation is one wherein the 1-N-arylpyrazole is acompound of the formula:

-   -   in which:    -   R₁ is a halogen atom, CN or methyl;    -   R₂ is S(O)_(n)R₃ or 4,5-dicyanoimidazol-2-yl or haloalkyl;    -   R₃ is alkyl, haloalkyl, haloalkenyl or haloalkynyl;    -   R₄ represents a hydrogen or halogen atom or an NR₅R₆,        S(O)_(m)R₇, C(O)R₇ or C(O)OR₇, alkyl, haloalkyl or OR₈ or an        —N═C(R₉)(R₁₀) group;    -   R₅ and R₆ independently represent a hydrogen atom or an alkyl,        haloalkyl, C(O)alkyl, S(O)_(r)CF₃ or alkoxycarbonyl group or R₅        and R₆ together may form a ring of 5 to 7 members;    -   R₇ represents an alkyl or haloalkyl substituent;    -   R₈ represents an alkyl or haloalkyl or a hydrogen;    -   R₉ represents an alkyl or a hydrogen atom;    -   R₁₀ represents an optionally substituted aryl or an optionally        substituted heteroaryl group;    -   R₁₁ and R₁₂ represent, independently of one another, hydrogen,        halogen CN or NO₂;    -   R₁₃ represents a halogen atom or a haloalkyl, haloalkoxy,        S(O)_(q)CF₃ or SF₅ group;    -   m, n, q and r represent, independently of one another, an        integer equal to 0, 1 or 2;    -   X represents a trivalent nitrogen atom or a C—R₁₂, the three        other valencies of the carbon atom forming part of the aromatic        ring;

with the proviso that, when R is methyl, then either R₃ is haloalkyl, R₄is NH₂,

-   -   R₁₁ is Cl, R₁₃ is CF₃ and X is N or else R₂ is        4,5-dicyanoimidazol-2-yl, R₄ is Cl, R₁₁ is Cl, R₁₃ is CF₃ and X        is C—Cl; and/or        More preferably, this invention provides for a parasitical        spot-on formulation wherein the 1-N-arylpyrazole in the        ectoparasitical combination is a compound of the formula (I)        wherein:    -   R₁ is a halogen atom, CN or methyl;    -   R₂ is S(O)_(n)R₃ or 4,5-dicyanoimidazol-2-yl or haloalkyl;    -   R₃ is C₁-C₆-alkyl or C₁-C₆-haloalkyl;    -   R₄ represents a hydrogen or halogen atom; or NR₅R₆, S(O)_(m)R₇,        C(O)R₇ or C(O)OR₇, alkyl, haloalkyl or OR₈ or —N═C(R₉) (R₁₀);    -   R₅ and R₆ independently represent a hydrogen atom or a C₁-C₆        alkyl, C₁-C₆-haloalkyl, C(O)C₁-C₆-alkyl, S(O)_(r)CF₃, C₁-C₆-acyl        or C₁-C₆-alkoxycarbonyl; R₅ and R₆ together may combine to form        a ring of 5 to 7 members, which may include one or two divalent        heteroatoms selected from the group consisting of oxygen or        sulphur;    -   R₇ represents a C₁-C₆-alkyl or C₁-C₆-haloalkyl;    -   R₈ represents a C₁-C₆-alkyl or C₁-C₆-haloalkyl or a hydrogen        atom;    -   R₉ represents a C₁-C₆-alkyl or a hydrogen atom;    -   R₁₀ represents an optionally substituted phenyl or optionally        substituted heteroaryl group wherein the substituents are        selected from the group consisting of halogen, OH, —O—C₁-C₆        alkyl, —S—C₁-C₆-alkyl, cyano or C₁-C₆-alkyl;    -   R₁₁ and R₁₂, independently of one another represent hydrogen,        halogen, CN or NO₂;    -   R₁₃ represents a halogen, C₁-C₆-haloalkyl, C₁-C₆-haloalkoxy,        S(O)_(q)Cl₃ or SF₅ group; and,    -   m, n, q and r independently of one another are 0, 1, or 2;

(b) the liquid carrier vehicle comprises a solvent and a cosolventwherein the solvent is selected from the group consisting of acetone,acetonitrile, benzyl alcohol, butyl diglycol, dimethylacetamide,dimethylformamide, dipropylene glycol n-butyl ether, ethylene glycolmonoethyl ether, monomethylacetamide, d ipropylene glycol monomethylether, liquid polyoxyethylene glycols, propylene glycol, 2-pyrrolidone,in particular N-methylpyrrolidone, diethylene glycol monoethyl ether,ethylene glycol, diethyl phthalate fatty acid esters, such as thediethyl ester or diisobutyl adipate, and a mixture of at least two ofthese solvents and the cosolvent is selected from the group consistingof ethanol, isopropanol or methanol; and

(c) a crystallization inhibitor selected from the group consisting of ananionic surfactant, a cationic surfactant, a non-ionic surfactant, anamine salt, an amphoteric surfactant or polyvinylpyrrolidone, polyvinylalcohols, copolymers of vinyl acetate and vinylpyrrolidone, polyethyleneglycols, benzyl alcohol, mannitol, glycerol, sorbitol,polyoxyethylenated sorbitan esters; lecithin, sodiumcarboxymethylcellulose, and acrylic derivatives, or a mixture of thesecrystallization inhibitors.

Especially preferred as spot-on formulations are those wherein the1-N-arylpyrazole derivative in the ectoparasitical combination is acompound wherein the ring formed by the divalent alkylene substituentrepresenting R₅ and R₆ and the nitrogen atom to which R₅ and R₆ areattached has 5, 6 or 7 members or wherein R₁ is CN, R₃ isC₁-C₆-haloalkyl, R₄ is NH₂, R₁₁, and R₁₂ are, independently of oneanother, hydrogen or halogen and R₁₃ is C₁-C₆-haloalkyl.

Most especially preferred 1-N-arylpyrazoles to be used in the inventivespot-on and pour-on formulations are:

(A)5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinylpyrazole;or

(B) 1-N-phenylpyrazole derivative of the formula:

Other 1-N-arylpyrazole derivatives to be used in the formulation to theinvention which are preferred are those of the formula (II)

wherein:

-   -   R₁₀₁ is cyano, —C(O)alkyl, C(S)NH₂, alkyl, haloalkyl, C(═NOH)NH₂        or C(═NNH₂)NH₂;    -   R₁₀₂ is S(O)_(n),R₁₀₃, alkenyl, haloalkenyl, cycloalkyl,        halocycloalkyl or alkynyl;    -   R₁₀₃ is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl or        haloalkynyl;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆, —N═C(R₁₀₅)—N(R₁₀₇)—R₁₀₈; or        —N(R₁₀₉)—C(R₁₀₅)=NR₁₀₆;    -   R₁₀₅ is hydrogen; alkyl; or alkyl substituted by halogen,        alkoxy, haloalkoxy or —S(O)_(m),R₁₀₅;    -   R₁₀₆ and R₁₀₇ each independently represent hydrogen, alkyl,        alkenyl or alkynyl, or alkyl substituted by one or more halogen,        alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, cyano or        —S(O)_(m),R₁₁₅; or alkyl substituted by phenyl or pyridyl each        of which is optionally substituted with one or more groups        selected from halogen, nitro and alkyl group; or    -   R₁₀₇ and R₁₀₈ may form together with the nitrogen to which they        are attached a 3- to 7-membered ring which may additionally        contain one or more heteroatoms selected from oxygen, nitrogen        or sulfur;    -   R₁₀₈ is alkoxy, haloalkoxy, amino, alkylamino, dialkylamino,        —C(O) R₁₁₄ or —S(O)_(t),R₁₁₀;    -   R₁₀₉, R₁₁₀ and R₁₁₄ are alkyl or haloalkyl;    -   R₁₁₁ and R₁₁₂ are independently selected from halogen, hydrogen,        CN and NO₂    -   R₁₁₃ is selected from halogen, haloalkyl, haloalkoxy,        —S(O)_(q),CF₃, and —SF₅;    -   R₁₁₅ is alkyl or haloalkyl;    -   X is selected from nitrogen and C—R₁₁₂;    -   Z is O, S(O)_(a)′; or NR₁₀₇;    -   a′, m′, n′ and q′ are independently selected from 0, 1, and 2;        and    -   t′ is 0, 1 or 2; and veterinary acceptable salts thereof.

Other preferred 1-N-arylpyrazole derivatives that may be included in theinventive formulations are those compounds of formula (III):

wherein:

-   -   R₂₀₁ is cyano, C(O)alkyl, C(S)NH₂, alkyl, C(═NOH)NH₂ or        C(═NNH₂)NH₂;    -   R₂₀₂ is S(O)_(h)R₂₀₃, alkenyl, haloalkenyl, cycloalkyl,        halocycloalkyl or alkynyl;    -   R₂₀₃ is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl or        haloalkynyl;    -   R₂₀₄ is —N(R₂₀₅)C(O)CR₂₀₆R₂₀₇R₂₀₈, —N(R₂₀₅)C(O)aryl, or        —N(R₂₀₅)C(O)OR₂₀₇;    -   R₂₀₅ is alkyl, haloalkyl, cycloalkyl, halocycloalkyl,        cycloalkylalkyl, halocycloalkylalkyl, alkoxyalkyl,        haloalkoxyalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl;    -   R₂₀₆ is hydrogen, halogen, alkoxy, haloalkoxy, alkoxyalkyl,        haloalkoxyalkyl, formyloxy, alkylcarbonyloxy,        haloalkylcarbonyloxy, alkylthio, haloalkylthio, alkylsulfinyl,        haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, alkylamino,        dialkylamino, haloalkylamino, di(haloalkyl)amino, cycloalkyloxy,        halocycloalkyloxy, alkoxyalkoxy, haloalkoxyalkoxy,        alkoxyalkoxyalkoxy, aryloxy, or arylalkoxy;    -   R₂₀₇ and R₂₀₈ are independently hydrogen, alkyl, haloalkyl,        cycloalkyl, or halocycloalkyl; or R₂₀₇ and R₂₀₈ may form        together with the carbon to which they are attached a 3- to        7-membered ring which additionally may contain one or more        heteroatoms selected from nitrogen, oxygen and sulfur;    -   X₁ is selected from nitrogen and C—R₂₁₂;    -   R₂₁₁, and R₂₁₂ are independently selected from halogen,        hydrogen, CN and NO₂;    -   R₂₁₃ is selected from halogen, haloalkyl, haloalkoxy,        —S(O)_(k)CF₃, and —SF₅;    -   and    -   h and k are independently selected from 0, 1, and 2;    -   and veterinary acceptable carrier, excipients and salts thereof.

A preferred class of compounds of formula (II) for use in the inventiveformulation is those wherein:

-   -   R₁₀₃ is cyano or alkyl;    -   R₁₀₂ is S(O)_(n),R₁₀₃;    -   R₁₀₃ is alkyl or haloalkyl;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆;    -   R₁₀₅ is hydrogen, alkyl or haloalkyl;    -   Z is O, S(O)_(a)′; or NR₁₀₇;    -   R₁₀₆ and R₁₀₇ are independently selected from hydrogen and        unsubstituted or substituted alkyl; or    -   R₁₀₆ and R₁₀₇ may form together with the nitrogen to which they        are attached a 3- to 7-membered ring which may additionally        contain one or more heteroatoms selected from oxygen, nitrogen        or sulfur; X is selected from nitrogen and C—R₁₁₂;    -   R₁₁₁ and R₁₁₂ are independently selected from halogen, hydrogen,        CN and NO₂;    -   R₁₁₃ is selected from halogen, haloalkyl, haloalkoxy,        —S(O)_(q),CF₃, and —SF₅;    -   a′, n′ and q′ are independently selected from 0, 1, and 2.

Preferably, R₁₀₆ is alkyl which is substituted by one or more halogen,alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, sulfide, sulfoxide,sulfone, or phenyl or pyridyl moieties of which each phenyl or pyridylmoiety is optionally substituted with one or more groups selected fromhalo, nitro, and alkyl.

Preferably, the 1-N-arylpyrazole has one or more of the followingfeatures:

-   -   R₁₀₁ is cyano;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆ and Z is —NR₁₀₇;    -   X is C—R₁₁₂; R₁₁₁ and R₁₁₂ represent a chlorine atom; and R₁₁₃        is CF₃, OCF₃, or —SF₅;    -   R₁₁₂ is —S(O)_(n),CF₃ and n is 0, 1, or 2.

A further preferred class of 1-N-arylpyrazoles that may be included inthe inventive formulations or approaches are those of formula IIwherein:

-   -   R₁₀₁ is cyano or alkyl; R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆; and R₁₀₅ is        hydrogen or C₁-C₃ alkyl.

The compounds of formula (II) preferably have one or more of thefollowing features:

-   -   R₁₀₁ is cyano or methyl;    -   R₁₀₃ is halomethyl (preferably CF₃);    -   R₁₁₁ and R₁₁₂ each independently represent a halogen atom;    -   X is C—R₁₁₂;    -   R₁₁₃ is haloalkyl (preferably CF₃ haloalkoxy (preferably OCF₃),        or —SF₅; or    -   n′ is 0, 1 or 2 (preferably 0 or 1).

A further preferred class of compounds of formula (II) for use in theinventive formulations and methods are those wherein:

-   -   R₁₀₁ is cyano;    -   R₁₀₂ is S(O)_(n),R₁₀₃;    -   R₁₀₃ is halomethyl;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆;    -   Z is NR₁₀₇;    -   R₁₀₅ is hydrogen or alkyl;    -   R₁₀₆ and R₁₀₇ each independently represent hydrogen, alkyl,        alkenyl or alkynyl; or alkyl substituted by one or more halogen,        alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, cyano or        —S(O)_(m)R₁₅; or alkyl substituted by phenyl or pyridyl which        rings are optionally substituted with one or more groups        selected from halogen, nitro and alkyl;    -   X is selected from nitrogen and C—R₁₁₂;    -   R₁₀₆ and R₁₁₂ each independently represent a halogen atom; R₁₁₃        is selected from haloalkyl, haloalkoxy and —SF₅; R₁₁₅ is alkyl        or haloalkyl; and    -   m′ and n′ are independently selected from 0, 1, and 2.

A further preferred class of compounds of formula (II) is that wherein:

-   -   R₁₀₁ is cyano;    -   R₁₀₂ is S(O)_(n),CF₃;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆ or —N═C(R₀₅)—N(R₁₀₇)—R₁₀₈;    -   Z is NR₁₀₇;    -   R₁₀₅ is hydrogen or alkyl;    -   R₁₀₆ and R₁₀₇ each independently represent hydrogen, alkyl,        alkenyl or alkynyl; or alkyl substituted by one or more halogen,        alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, cyano or        —S(O)R₁₁₅; or methyl substituted by phenyl or pyridyl which        rings are optionally substituted with one or more groups        selected from halogen, nitro and alkyl;    -   R₁₀₈ is alkoxy, haloalkoxy, amino, alkylamino, dialkylamino or        —S(O)_(t),R₁₁₀;    -   X is selected from nitrogen and C—R₁₁₂;    -   R₁₀₉, R₁₁₀ and R₁₁₄ independently represent alkyl or haloalkyl;    -   R₁₁₁ and R₁₁₂ each represent a chlorine atom;    -   R₁₁₃ is CF₃ or —SF₅; and    -   m′ and n′ are 0, 1 or 2; and t′ is 0 or 2.

A further preferred class of compounds of formula (II) are thosewherein:

-   -   R₁₀₁ is cyano;    -   R₁₀₂ is S(O)_(n1)CF₃;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆;    -   Z is NR₁₀₇;    -   R₁₀₅ is hydrogen or methyl;    -   R₁₀₆ and R₁₀₇ each independently represent hydrogen, alkyl,        alkenyl or alkynyl; or alkyl substituted by one or more halogen,        alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, cyano or        —S(O)_(m),R₁₁₅; or alkyl substituted by phenyl or pyridyl which        rings are optionally substituted with one or more groups        selected from halogen, nitro and alkyl;    -   X is C—R₁₁₂    -   R₁₁₁ and R₁₁₂ each represent a chlorine atom;    -   R₁₁₃ is CF₃ or —SF₅;    -   m′ is zero, one or two; and    -   n′ is 0 or 1.

A further preferred class of compounds of formula (II) is those wherein:

-   -   R₁₀₁ is cyano;    -   R₁₀₂ is S(O)_(n),CF₃;    -   R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆;    -   Z is NR₁₀₇;    -   R₁₀₅ and R₁₀₇ each represent a hydrogen atom;    -   R₁₀₆ is alkyl or haloalkyl;    -   X is C—R₁₁₂;    -   R₁₁₁ and R₁₁₂ each represent a chlorine atom;    -   R₁₁₃ is CF₃ or —SF₅; and    -   n′ is 0.

Compounds of formula (III) which are preferred according to the presentinvention are those wherein:

-   -   R₂₀₁ is cyano;    -   R₂₀₂ is S(O)_(h)R₂₀₃;    -   R₂₀₃ is alkyl or haloalkyl;    -   R₂₀₄ is —N(R₂₀ ₅)C(O)CR₂₀₆R₂₀₇R₂₀₈;    -   R₂₀₅ is alkyl, haloalkyl, cycloalkyl, cycloalkylalkyl and        halocycloalkylalkyl;    -   R₂₀₆ is alkoxy, haloalkoxy, or hydrogen;    -   R₂₀₇ and R₂₀₈ are independently hydrogen, alkyl, or haloalkyl;        or    -   R₂₀₇ and R₂₀₈ may form together with the carbon to which they        are attached to a 3- to 7-membered ring which additionally may        contain one or more heteroatoms selected from nitrogen, oxygen        and sulfur;    -   X₁ is selected from nitrogen and C—R₂₁₂;    -   R₂₁₁ and R₂₁₂ are independently selected from halogen, hydrogen,        CN and NO₂;    -   R₂₁₃ is selected from halogen, haloalkyl, haloalkoxy,        —S(O)_(k)CF₃, and —SF₅;    -   and    -   h and k are independently selected from 0, 1, and 2.

A preferred group of compounds of formula (III) is that wherein the ringwhich is formed by R₂₀₇ and R₂₀₈ contains one or more heteroatoms, morepreferably one oxygen atom.

The compounds of formula (III) of the present invention preferably haveone or more of the following features:

-   -   R₂₀₁ is cyano;    -   R₂₀₃ is halomethyl, preferably CF₃;    -   R₂₁₁ and R₂₁₂ are independently halogen;    -   X₁ is C—R₂₁₂;    -   R₂₁₃ is haloalkyl, haloalkoxy or —SF₅; or    -   h is 0 or 1, or 2, preferably 0 or 1.

A preferred class of compounds that wherein R₂₀₄ isN(R₂₀₅)C(O)CR₂₀₆R₂₀₇R₂₀₈.

Another preferred class of compounds that wherein R₂₀₄ isN(R₂₀₅)C(O)aryl.

Another preferred class of compounds that wherein R₂₀₄ isN(R₂₀₅)C(O)OR₂₀₇.

Preferably R₂₀₅ is C₁-C₄ alkyl, more preferably C₁-C₂ alkyl, mostpreferably methyl.

Preferably R₂₀₆ is alkoxy, most preferably methoxy, ethoxy or propoxy.

Preferably R₂₀₇ and R₂₀₈ are both hydrogen.

Another especially preferred group of 1-N-arylpyrazole derivatives is4-thiocarbonylpyrazole derivatives of the formula:

in which

-   -   R³⁰¹ is H₂N—C(S)—,    -   R³⁰² is halogenoalkyl, halogenoalkenyl or halogenoalkynyl,    -   R³⁰³ is hydrogen, amino or one of the following groups:

where

-   -   R³⁰⁴ represents alkyl, halogenoalkyl, alkoxyalkyl or in each        case optionally substituted phenyl or pyridyl,    -   R³⁰⁵ represents hydrogen or alkyl,    -   R³⁰⁶ represents hydrogen, alkyl or in each case optionally        substituted phenyl or pyridyl and    -   R³⁰⁷ represents alkyl, alkenyl, alkinyl, formyl, alkylcarbonyl,        halogenoalkylcarbonyl or alkoxycarbonyl;    -   Ar represents in each case optionally substituted phenyl or        pyridyl and n represents a number 0, 1 or 2.

Especially preferred derivatives of formula (IV) are those wherein

-   -   R³⁰¹ represents H₂N—C(S)—;    -   R³⁰² preferably represents (C₁-C₆)-halogenoalkyl having 1 to 12        halogen atoms; (C₂-C₆)-halogenoalkenyl having 1 to 8 halogen        atoms or (C₁-C₆)-halogenoalkinyl having 1 to 6 halogen atoms;    -   R³⁰³ preferably represents hydrogen, amino or one of the        following groups:

wherein:

-   -   R³⁰⁴ represents (C₁-C₆)-alkyl, (C₁-C₆)-halogenoalkyl having 1 to        3 halogen atoms, (C₁-C₆)-alkoxy-(C₁-C₆)-alkyl, or represents        phenyl or pyridyl, each of which is optionally monosubstituted        to trisubstituted by identical or different substituents from        the group consisting of cyano, nitro, halogen, C₁-C₆-alkyl,        C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₄-halogenoalkyl, C₁-C₄        halogenoalkoxy or C₁-C₄-halogenoalkylthio having in each case 1        to 5 halogen atoms,    -   R³⁰⁵ represents hydrogen or (C₁-C₆)-alkyl,    -   R³⁰⁶ represents hydrogen, (C₁-C₆)-alkyl, phenyl which is        optionally monosubstituted to trisubstituted by identical or        different substituents from the group consisting of cyano,        nitro, halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio,        C₁-C₄-halogenoalkyl, C₁-C₄-halogenoalkoxy or        C₁-C₄-halogenoalkylthio having in each case 1 to 5 halogen atoms        or hydroxyl, or represents pyridyl which is substituted by        cyano, nitro, halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy,        C₁-C₆-alkylthio, C₁-C₄-halogenoalkyl, C₁-C₄-halogenoalkoxy or        C₁-C₄-halogenoalkylthio having in each case 1 to 5 halogen        atoms, and    -   R³⁰⁷ represents (C₁-C₆)-alkyl, (C₂-C₆)-alkenyl, (C₂-C₆)-alkynyl,        formyl, (C₁-C₆)-alkylcarbonyl, (C₁-C₆)-halogenoalkylcarbonyl        having 1 to 6 halogen atoms or (C₁-C₆)-alkoxycarbonyl;    -   Ar preferably represents phenyl or pyridyl, each of which is        optionally monosubstituted to trisubstituted by identical or        different substituents from the group consisting of halogen        halogeno(C₁-C₆)alkyl, halogeno(C₁-C₆) alkylthio,        halogeno(C₁-C₆)alkoxy, (C₁-C₆)alkoxy, methoxy, hydrazine,        (C₁-C₆)-dialkylhydrazino, amino, (C₁-C₆)alkylamino,        di(C₁-C₆)alkylamino, (C₁-C₆) alkylimino, cyano, (C₁-C₆)alkylthio        or the group

-   -   in which    -   R³⁰⁸ and R³⁰⁹ are identical or different and represent hydrogen        or (C₁-C₆)-alkyl    -   n¹¹¹ preferably represents a number 0, 1 or 2.    -   R³⁰¹ represents H₂N—C(S)—;    -   R³⁰² particularly preferably represents (C₁-C₄)-halogenoalkyl        having 1 or 9 identical or different halogen atoms from the        group consisting of fluorine, chlorine and bromine,        (C₂-C₄)-halogenoalkenyl having 1 to 5 identical or different        halogen atoms from the group consisting of fluorine, chlorine or        bromine or (C₂-C₄)-halogenoalkynyl having 1 to 5 identical or        different halogen atoms from the group consisting of fluorine,        chlorine and bromine; R³⁰³ especially preferably represents        hydrogen, amino or one of the following groups:

where

-   -   R³⁰⁴ represents (C₁-C₄)-alkyl, (C₁-C₄)-halogenoalkyl having 1-3        halogen atoms, (C₁-C₄)-alkoxy(C₁-C₂)-alkyl, or phenyl which is        optionally monosubstituted to trisubstituted by identical or        different substituents from the group consisting of hydroxyl,        cyano, nitro, halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy,        (C₁-C₂-halogenoalkyl, C₁-C₂-halogenoalkoxy or        C₁-C₂-halogenoalkylthio having in each case 1 to 3 halogen        atoms,    -   R³⁰⁵ represents hydrogen or (C₁-C₄)-alkyl,    -   R³⁰⁶ represents hydrogen, (C₁-C₄)-alkyl or phenyl which is        optionally monosubstituted or disubstituted by identical or        different substituents from the group consisting of hydroxyl,        cyano, nitro, halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy,        C₁-C₂-halogenoalkyl, C₁-C₂ halogenoalkoxy or C₁-C₂        halogenoalkylthio having in each case 1 to 3 halogen atoms, in        particular 4-hydroxy-3-methoxy-phenyl, and    -   R³⁰⁷ represents (C₁-C₄)-alkyl, (C₂-C₄)-alkenyl, (C₂-C₄)-alkynyl,        formyl, (C₁-C₄)-alkylcarbonyl, (C₁-C₄,)-halogenoalkylcarbonyl        having 1 to 5 identical or different halogen atoms from the        group consisting of fluorine, chlorine or bromine or        (C₁-C₄)-alkoxycarbonyl;    -   Ar especially preferably represents phenyl or pyridyl, each of        which is optionally monosubstituted to trisubstituted by        identical or different substituents from the group consisting of        fluorine, chlorine, trifluoromethyl, trifluoromethylthio,        trifluoromethoxy, methoxy, hydrazine, dimethylhydrazino, amino,        methylamino, dimethylamino, iminomethyl, cyano, methylthio or        the group

where

-   -   R³⁰⁸ and R³⁰⁹ are identical or different and represent hydrogen        or (C₁-C₄)-alkyl;    -   n¹¹¹ especially preferably represents a number 0, 1 or 2.

Compounds of formula (IV) which are most preferably preferred are thosewhere

-   -   R³⁰¹ represents H₂N—C(S)—;    -   R³⁰² most preferably represents one of the following groups:        -   —CF₃, —CHF₂—CF₂—CH₃—CF₃—CHF₂, —CF₂CHFCl, —CH₂—CF₃,            —CH₂CF₂CI, —CH₂—CF₂—CHF₂, —CF₂—CFC₁-CF₃, —C(Cl)(CF₃)—CF₂Cl,            —C(Cl)(CF₃)—CHCl—CF₃, —C(CF₃)═CCl₂    -   R³⁰³ most preferably represents hydrogen, amino or one of the        groups:

Ar most preferably represents

(1) phenyl which is disubstituted or trisubstituted by identical ordifferent substituents, where fluorine or chlorine occupies the2-position, trifluoromethyl the 4-position and fluorine, chlorine,cyano, methoxy, methylthio, trifluoromethyl, trifluoromethoxy,trifluoromethylthio or hydrazino the 6-position; or

(2) a 2-pyridyl substituent which is substituted in the 4-position bytrifluoromethyl and in the 6-position by fluorine or chlorine.

-   -   n¹¹¹ most preferably represents one of the integers 0, 1 or 2. A        most especially preferred compound is one wherein R³⁰² is —CF₃,        R³⁰³ is amino, Ar is a phenyl which is trisubstituted and the        substituents are a 2-position chloro group, a 4-position        trifluoromethyl group and a 6-position chloro group, and n¹¹¹ is        1.

Especially preferred compounds are those of the formulae.

Other preferred 1-N-arylpyrazoles include the following compounds:

Especially preferred 1-N-arylpyrazoles derivative in addition tofipronil include fipronil thio

and fipronil sulfone

In addition to the patent discussing 1-N-arylpyrazoles derivativesdiscussed previously, one skilled in the art could make these compoundsby adopting procedures described in DE 19928155, DE 19853560, WO2000031043, DE 19650197, WO 9824769, U.S. Pat. No. 6,265,430, U.S.2001007876, all of which are herein incorporated by reference.

The alkyl groups of the definition of the compounds (1) of the formula(I) generally comprise from 1 to 6 carbon atoms. The ring formed by R₅and R₆ and the nitrogen atom to which they are attached is generally a5-, 6- or 7-membered ring.

Unless otherwise specified, alkyl and alkoxy groups are generally loweralkyl and alkoxy groups, that is having from one to six carbon atoms,preferably from one to four carbon atoms. Generally, the haloalkyl,haloalkoxy and alkylamino groups have from one to four carbon atoms. Thehaloalkyl and haloalkoxy groups can bear one or more halogen atoms;preferred groups of this type include —CF₃ and —OCF₃. Cycloalkyl groupsgenerally have from 3 to 6 carbon atoms, preferably from 3 to 5 carbonatoms, and may be substituted by one or more halogen atoms. Alkenyl,haloalkenyl, alkynyl, and haloalkynyl groups generally contain from 3 to5 carbon atoms. By the term aryl is generally meant phenyl, pyridyl,furyl, and thiophenyl, each of which is optionally substituted by one ormore halogen, alkyl, haloalkyl, nitro, alkoxy, haloalkoxy, hydroxy,amino, alkylamino or dialkylamino. In compounds of formulae (1) to(III), by the term substituted alkyl is meant alkyl which is substitutedby, for example, one or more halogen, alkoxy, haloalkoxy, amino,alkylamino, dialkylamino, cyano or —S(O)_(m)R₁₁₅; or alkyl substitutedby phenyl or pyridyl each of which is optionally substituted with one ormore groups selected from halogen, nitro and alkyl; wherein R₁₁₅ isalkyl or haloalkyl and m is zero, one or two. Preferably in compounds offormula (I), alkyl groups are generally substituted by from one to fivehalogen atoms, preferably from one to three halogen atoms. Chlorine andfluorine atoms are preferred.

Compounds of formula wherein R₁₀₄ is —N═C(R₁₀₅)-Z-R₁₀₆, Z is NR₁₀₇ andR₁₀₆ represent a hydrogen atom may exist as the tautomeric double bondisomer form —NH—C(R₁₀₅)═N—R₁₀₇. It is to be understood that both suchforms are embraced by the present invention.

In compounds of formula (III) the following examples of substituents areprovided:

An example of cycloalkylalkyl is cyclopropylmethyl; an example ofcycloalkoxy is cyclopropyloxy;

An example of alkoxyalkyl is CH₃OCH₂—;

An example of alkoxyalkoxy is CH₃OCH₂O—;

An example of alkoxyalkoxyalkoxy is CH₃OCH₂OCH₂O—;

An example of aryloxy is the phenoxy group; and

An example of the arylalkoxy group is benzyloxy or 2-phenylethoxy.

Generally, in dialkylamino or di(haloalkyl)amino groups, the alkyl andhaloalkyl groups on nitrogen may be chosen independently of one another.

A preferred class of compounds of formula (I) comprises the compoundssuch that R₁ is CN, R₃ is haloalkyl, R₄ is NH₂, R₁₁ and R₁₂ are,independently of one another, a halogen atom and R₁₃ is haloalkyl.Preferably still, X is C—R₁₂. A compound of formula (I) which is veryparticularly preferred in the invention is5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinylpyrazoleor fipronil.

Compounds of formulae (I)-(III) can be prepared according to one orother of the processes described in Patent Applications WO 87/3781,93/6089 and 94/21606, and 00/59862 or European Patent Application295,117 or any other process coming within the competence of a personskilled in the art who is an expert in chemical synthesis. For thechemical preparation of the products of the invention, a person skilledin the art is regarded as having at his disposal, inter alia, the entirecontents of “Chemical Abstracts” and of the documents which are citedtherein.

As discussed above, amitraz is well known in the art and can be obtainedfrom commercial source.

IGR compounds are another class of insecticides or acaricides, which areprovided for in the bait formulations in this invention. Compoundsbelonging to this group are well known to the practitioner and representa wide range of different chemical classes. These compounds all act byinterfering with the development or growth of the insect pests.Compounds with an ovicidal and/or larvicidal effect on the immaturestages of various ectoparasites are already known, for example from U.S.Pat. No. 5,439,924. Among these compounds described are those IGRcompounds which act either by blocking the development of the immaturestages (eggs and larvae) into adult stages, or by inhibiting thesynthesis of chitin. Insect growth regulators are described, forexample, in U.S. Pat. No. 3,748,356; U.S. Pat. No. 3,818,047; U.S. Pat.No. 4,225,598; U.S. Pat. No. 4,798,837; and U.S. Pat. No. 4,751,225, aswell as in EP 179,022 or U.K. 2,140,010. French Patent No. A-2,713,889generally describes an IGR combination comprising at least one compoundwith juvenile hormone activity and chitin synthesis inhibitors, with atleast one of three N-arylpyrazole compounds, in particular fipronil, tocontrol many harmful insects belonging to very varied orders.

Examples of IGR compounds which may be used in this invention includecompounds which mimic juvenile hormones, in particular:

-   -   azadirchtin (Agridyne)    -   diofenolan (Novartis)    -   fenoxycarb (Novartis)    -   hydroprene (Novartis)    -   kinoprene (Novartis)    -   methoprene (Novartis)    -   pyriproxyfen (Sumitomo/Mgk)    -   tetrahydroazadirachtin (Agridyne)    -   4-chloro-2-(2-chloro-2-methylpropyl)-5-(6-iodo-3-pyridylmethoxy)pyridizin-3(2H)-one        and chitin-synthesis inhibitors, in particular:    -   chlorfluazuron (Ishihara Sangyo)    -   cyromazine (Novartis)    -   diflubenzuron (Solvay Duphar)    -   fluazuron (Novartis)    -   flucycloxuron (Solvay Duphar)    -   flufenoxuron (Cyanamid)    -   hexaflumuron (Dow Elanco)    -   lufenuron (Novartis)    -   tebufenozide (Rohm & Haas)    -   teflubenzuron (Cyanamid)    -   triflumuron (Bayer).        These compounds are defined by their international common name        (The Pesticide Manual, 10^(th) edition, 1994, Ed. Clive Tomlin,        Great Britain).

Chitin-synthesis inhibitors also include compounds such as1-(2,6-difluorobenzoyl)-3-(2-fluoro-4-((trifluoromethyl))phenylurea,1-(2,6-difluorobenzoyl)-3-(2-fluoro-4-(1,1,2,2-tetrafluoroethoxy))phenylureaand 1-(2,6-difluorobenzoyl)-3-(2-fluoro-4-trifluoro-methyl)phenylurea.Novaluron (Isagro, Italian company) is also an example of an IGRcompound.

Preferred IGR compounds include methoprenes, pyriproxyfens, hydroprene,cyromazine, lufenuron,1-(2,6-difluorobenzoyl)-3-(2-fluoro-4-(trifluoromethyl)phenylurea andnovaluron.

Other class compounds which maybe combined with the inventiveectoparasitical combination include avermectin and milbemycinderivatives, pyrethroids, benzamidazoles and imidazoles. Preferredavermectins or milbemycins include doramectin, enamectin, abamectin,eprinomectin, ivermectin, selamectin, moxidectin and milbemycin oxime.Preferred pyrethroids include the pyrethrins, permethrin, resmethrin andsumithrin. Preferred benzimidazole include albendazole, fenbenazole,mebendazole, oxibendazole and triclabendazole. A preferredimidazoleothiazole is levamisole. The amount of these compounds to beincluded with the inventive ectoparasitical combination depends on thetype of animal and the degree of infestation. The amounts of thesecompounds are easily determined by one skilled in the art.Representative amounts include 0.001 mg/kg to 100 mg/kg, with theavermectins having preferred range of 0.001 mg/kg to 10 mg/kg and theother classes from 0.1 mg/kg to 100 mg/kg.

Administration of the inventive formulation may be intermittent in timeand may be administered daily, weekly, biweekly, monthly, bimonthly,quarterly, or even for longer durations of time. The time period betweentreatments depends upon factors such as the parasite(s) being treated,the degree of infestation, the type of animal, mammal or bird, and theenvironment where it resides. It is well within the skill level of thepractitioner to determine a specific administration period for aparticular situation. This invention contemplates a method forpermanently combating a parasite in an environment in which the animalis subjected to strong parasitic pressure where the administration is ata frequency far below a daily administration in this case. For example,it is preferable for the treatment according to the invention to becarried out monthly on mammals, such as on dogs and on cats.

Spot-on formulations may be prepared by dissolving the activeingredients into the pharmaceutically or veterinary acceptable vehicle.Alternatively, the spot-on formulation can be prepared by encapsulationof the active ingredient to leave a residue of the therapeutic agent onthe surface of the animal. These formulations will vary with regard tothe weight of the therapeutic agent in the combination depending on thespecies of host animal to be treated, the severity and type of infectionand the body weight of the host. The compounds may be administeredcontinuously, particularly for prophylaxis, by known methods. Generally,a dose of from about 0.001 to about 10 mg per kg of body weight given asa single dose or in divided doses for a period of from 1 to 5 days willbe satisfactory but, of course, there can be instance where higher orlower dosage ranges are indicated and such are within the scope of thisspecific administration period for a particular situation. Thisinvention contemplates a method for combating mosquitoes in anenvironment in which the animal is subjected to strong mosquito pressurewhere the administration is at a frequency far below a dailyadministration in this case. For example, it is preferable for thetreatment according to the invention to be carried out monthly on dogsand on cats and or birds.

Spot-on and pour-on formulations may be prepared by dissolving theactive ingredients into the pharmaceutically or veterinary acceptablevehicle. Alternatively, the spot-on formulation can be prepared byencapsulation of the active ingredient to leave a residue of thetherapeutic agent on the surface of the animal. These formulations willvary with regard to the weight of the therapeutic agent in thecombination depending on the species of host animal to be treated, theseverity and type of infection and the body weight of the host. Thecompounds may be administered continuously, particularly forprophylaxis, by known methods. Generally, a dose of from about 0.001 toabout 100 mg per kg of body weight of 1-N-arylpyrazole and 0.01 to about100 mg/kg of amitraz given as a single dose or in divided doses for aperiod of from 1 to 5 days will be satisfactory but, of course, therecan be instance where higher or lower dosage ranges are indicated andsuch are within the scope of this invention. It is well within theroutine skill of the practitioner to determine a particular dosingregimen for a specific host and parasite.

Preferably, a single formulation containing the 1-N-arylpyrazolederivative is in a substantially liquid carrier and is in a form whichmakes possible a single application or an application repeated a smallnumber of times. The formulation will be administered to the animal overa highly localized region of the animal, preferably between the twoshoulders. It is well within the routine skill of the practitioner todetermine a particular dosing regimen for a specific host and parasite.Most preferably, this localized region has a surface area of less than10 cm², especially between 5 and 10 cm² area. Remarkably, it has beendiscovered that such a formulation is highly effective against both thetargeted parasites.

The treatment is preferably carried out so as to administer to the host,on a single occasion, a dose containing between about 0.001 and about100 mg/kg of a compound of formula (II).

The amount of compounds of 1-N-aylpyrazole for animals which are smallin size is preferably greater than about 0.01 mg and in a particularlypreferred way between about 1 and about 50 mg/kg of weight of animal.

It also may be preferable to use controlled-release formulations.

This invention also provides for a method for cleaning the coats and theskin of animals by removal of the parasites which are present and oftheir waste and excreta. The animals treated thus exhibit a coat whichis more pleasing to the eye and more pleasant to the touch.

The invention also relates to such a method with a therapeutic aimintended for the treatment and prevention of parasitoses havingpathogenic consequences.

In another preferred embodiment this provides for a composition forcombating fleas in small mammals, in particular dogs and cats,characterized in that it contains at least one of formula (II) asdefined above.

The formulations of the present invention provide for the topicaladministration of a concentrated solution, suspension, microemulsion oremulsion for intermittent application to a spot on the animal, generallybetween the two shoulders (solution of spot-on type). It has beendiscovered that the inventive formulations are especially active againstparasites when the formulations are applied to animals, such as mammals,especially dogs, cats, sheep, pigs, cattle and horses and birds,especially chickens, turkeys and quails. The ectoparasitical combinationcan advantageously be present in this formulation in a proportion ofabout 1 to about 20%, preferably of about 5 to about 15% (percentages asweight by volume=W/V). The liquid carrier vehicle comprises apharmaceutically or veterinary acceptable organic solvent and optionallyan organic cosolvent.

Also contemplated are the pharmaceutically or veterinary acceptable acidor base salts, where applicable, of the active compounds provided forherein. The term “acid” contemplates all pharmaceutically or veterinaryacceptable inorganic or organic acids. Inorganic acids include mineralacids such as hydrohalic acids, such as hydrobromic and hydrochloricacids, sulfuric acids, phosphoric acids and nitric acids. Organic acidsinclude all pharmaceutically or veterinary acceptable aliphatic,alicyclic and aromatic carboxylic acids, dicarboxylic acidstricarboxylic acids and fatty acids. Preferred acids are straight chainor branched, saturated or unsaturated C₁-C₂₀ aliphatic carboxylic acids,which are optionally substituted by halogen or by hydroxyl groups, orC₆-C₁₂ aromatic carboxylic acids. Examples of such acids are carbonicacid, formic acid, fumaric acid, acetic acid, propionic acid,isopropionic acid, valeric acid, α-hydroxy acids, such as glycolic acidand lactic acid, chloroacetic acid, benzoic acid, methane sulfonic acid,and salicylic acid. Examples of dicarboxylic acids include oxalic acid,malic acid, succinic acid, tartaric acid and maleic acid. An example ofa tricarboxylic acid is citric acid. Fatty acids include allpharmaceutically or veterinary acceptable saturated or unsaturatedaliphatic or aromatic carboxylic acids having 4 to 24 carbon atoms.Examples include butyric acid, isobutyric acid, sec-butyric acid, lauricacid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenicacid, and phenylsteric acid. Other acids include gluconic acid,glycoheptonic acid and lactobionic acid.

The term “base” contemplates all pharmaceutically or veterinaryacceptable inorganic or organic bases. Such bases include, for example,the alkali metal and alkaline earth metal salts, such as the lithium,sodium, potassium, magnesium or calcium salts. Organic bases include thecommon hydrocarbyl and heterocyclic amine salts, which include, forexample, the morpholine and piperidine salts.

The organic solvent for the liquid carrier vehicle will preferably havea dielectric constant of between about 10 and about 35, preferablybetween about 20 and about 30, the content of this solvent in theoverall composition preferably representing the remainder to 100% of thecomposition. It is well within the skill level of the practitioner toselect a suitable solvent on the basis of these parameters.

The organic cosolvent for the liquid carrier vehicle will preferablyhave a boiling point of less than about 100° C., preferably of less thanabout 80° C., and will have a dielectric constant of between about 10and about 40, preferably between about 20 and about 30; this cosolventcan advantageously be present in the composition according to aweight/weight (W/W) ratio with respect to the solvent of between about1/15 and about 1/2; the cosolvent is volatile in order to act inparticular as drying promoter and is miscible with water and/or with thesolvent. Again, it is well within the skill level of the practitioner toselect a suitable solvent on the basis of these parameters.

The organic solvent for the liquid carrier includes the commonlyacceptable organic solvents known in the formulation art. These solventsmay be found, for example, in Remington Pharmaceutical Science, 16^(th)Edition (1986). These solvents include, for example, acetone, ethylacetate, methanol, ethanol, isopropanol, dimethylformamide,dichloromethane or diethylene glycol monoethyl ether (Transcutol). Thesesolvents can be supplemented by various excipients according to thenature of the desired phases, such as C₈-C₁₀ caprylic/caprictriglyceride (Estasan or Miglyol 812), oleic acid or propylene glycol.

The liquid carrier may also comprise a microemulsion. Microemulsions arealso well suited as the liquid carrier vehicle. Microemulsions arequaternary systems comprising an aqueous phase, an oily phase, asurfactant and a cosurfactant. They are translucent and isotropicliquids.

Microemulsions are composed of stable dispersions of microdroplets ofthe aqueous phase in the oily phase or conversely of microdroplets ofthe oily phase in the aqueous phase. The size of these microdroplets isless than 200 nm (1000 to 100,000 nm for emulsions). The interfacialfilm is composed of an alternation of surface-active (SA) andco-surface-active (Co-SA) molecules which, by lowering the interfacialtension, allows the microemulsion to be formed spontaneously.

The oily phase can in particular be formed from mineral or vegetableoils, from unsaturated polyglycosylated glycerides or fromtriglycerides, or alternatively from mixtures of such compounds. Theoily phase preferably comprises triglycerides and more preferablymedium-chain triglycerides, for example C₈-C₁₀ caprylic/caprictriglyceride. The oily phase will represent, in particular, from about 2to about 15%, more particularly from about 7 to about 10%, preferablyfrom about 8 to about 9%, V/V of the microemulsion.

The aqueous phase includes, for example water or glycol derivatives,such as propylene glycol, glycol ethers, polyethylene glycols orglycerol. Propylene glycol, diethylene glycol monoethyl ether anddipropylene glycol monoethyl ether are especially preferred. Generally,the aqueous phase will represent a proportion from about 1 to about 4%V/V in the microemulsion.

Surfactants for the microemulsion include diethylene glycol monoethylether, dipropyelene glycol monomethyl ether, polyglycolysed C₈-C₁₀glycerides or polyglyceryl-6 dioleate. In addition to these surfactants,the cosurfactants include short-chain alcohols, such as ethanol andpropanol.

Some compounds are common to the three components discussed above, i.e.,aqueous phase, surfactant and cosurfactant. However, it is well withinthe skill level of the practitioner to use different compounds for eachcomponent of the same formulation.

The cosurfactant to surfactant ratio will preferably be from about 1/7to about 1/2. There will preferably be from about 25 to about 75% V/V ofsurfactant and from about 10 to about 55% V/V of cosurfactant in themicroemulsion.

Likewise, the co-solvents are also well known to a practitioner in theformulation art. Preferred co-solvents are those which is a promoter ofdrying and include, for example, absolute ethanol, isopropanol(2-propanol) or methanol.

The crystallization inhibitor can in particular be present in aproportion of about 1 to about 20% (W/V), preferably of about 5 to about15%. The inhibitor preferably corresponds to the test in which 0.3 ml ofa solution comprising 10% (W/V) of the compound of formula (I) in theliquid carrier and 10% of the inhibitor are deposited on a glass slideat 20° C. and allowed to stand for 24 hours. The slide is then observedwith the naked eye. Acceptable inhibitors are those whose additionprovides for few or no crystals, and in particular less than 10crystals, preferably 0 crystals.

Although this is not preferred, the formulation can optionally comprisewater, in particular in a proportion of 0 to about 30% (volume by volumeV/V), in particular of 0 to about 5%.

The formulation can also comprise an antioxidizing agent intended toinhibit oxidation in air, this agent being in particular present in aproportion of about 0.005 to about 1% (W/V), preferably of about 0.01 toabout 0.05%.

Crystallization inhibitors which can be used in the invention include:

-   -   polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl        acetate and of vinylpyrrolidone, polyethylene glycols, benzyl        alcohol, mannitol, glycerol, sorbitol or polyoxyethylenated        esters of sorbitan; lecithin or sodium carboxymethylcellulose;        or acrylic derivatives, such as methacrylates and others,    -   anionic surfactants, such as alkaline stearates, in particular        sodium, potassium or ammonium stearate; calcium stearate or        triethanolamine stearate; sodium abietate; alkyl sulphates, in        particular sodium lauryl sulphate and sodium cetyl sulphate;        sodium dodecylbenzenesulphonate or sodium dioctyl        sulphosuccinate; or fatty acids, in particular those derived        from coconut oil,    -   cationic surfactants, such as water-soluble quaternary ammonium        salts of formula N⁺R′R″R′″R″″Y⁻, in which the R radicals are        identical or different optionally hydroxylated hydrocarbon        radicals and Y⁻ is an anion of a strong acid, such as halide,        sulphate and sulphonate anions; cetyltrimethylammonium bromide        is one of the cationic surfactants which can be used,    -   amine salts of formula N⁺R′R″ R′″, in which the R radicals are        identical or different optionally hydroxylated hydrocarbon        radicals; octadecylamine hydrochloride is one of the cationic        surfactants which can be used,    -   non-ionic surfactants, such as optionally polyoxyethylenated        esters of sorbitan, in particular Polysorbate 80, or        polyoxyethylenated alkyl ethers; polyethylene glycol stearate,        polyoxyethylenated derivatives of castor oil, polyglycerol        esters, polyoxyethylenated fatty alcohols, polyoxyethylenated        fatty acids or copolymers of ethylene oxide and of propylene        oxide,    -   amphoteric surfactants, such as substituted lauryl compounds of        betaine,    -   or preferably a mixture of at least two of the compounds listed        above.

In a particularly preferred embodiment, a crystallization inhibitor pairwill be used. Such pairs include, for example, the combination of afilm-forming agent of polymeric type and of a surface-active agent.These agents will be selected in particular from the compounds mentionedabove as crystallization inhibitor.

Particularly preferred film-forming agents of polymeric type include:

-   -   the various grades of polyvinylpyrrolidone,    -   polyvinyl alcohols, and    -   copolymers of vinyl acetate and of vinylpyrrolidone.

Especially preferred surface-active agents, include those made ofnon-ionic surfactants, preferably polyoxyethylenated esters of sorbitanand in particular the various grades of polysorbate, for examplePolysorbate 80.

The film-forming agent and the surface-active agent can in particular beincorporated in similar or identical amounts within the limit of thetotal amounts of crystallization inhibitor mentioned elsewhere.

The pair thus constituted secures, in a noteworthy way, the objectivesof absence of crystallization on the coat and of maintenance of thecosmetic appearance of the fur, that is to say without a tendencytowards sticking or towards a sticky appearance, despite the highconcentration of active material.

Particularly preferred antioxidizing agents are those conventional inthe art and include, for example, butylated hydroxyanisole, butylatedhydroxytoluene, ascorbic acid, sodium metabisulphite, propyl gallate,sodium thiosulphate or a mixture of not more than two of them.

The formulation adjuvants discussed above are well known to thepractitioner in this art and may be obtained commercially or throughknown techniques. These concentrated compositions are generally preparedby simple mixing of the constituents as defined above; advantageously,the starting point is to mix the active material in the main solvent andthen the other ingredients or adjuvants are added.

The volume applied can be of the order of about 0.3 to about 1 ml,preferably of the order of about 0.5 ml, for cats and of the order ofabout 0.3 to about 5 ml for dogs, depending on the weight of the animal.

The pour-on solutions according to the invention, which areadvantageously oily, generally comprise a diluent or vehicle and also asolvent (organic solvent) for the compound of formula (II) if the latteris not soluble in the diluent. Low concentrations of from about 0.05 toabout 10% weight/volume, more particularly from about 0.1 to about 2%,are preferred. Optimally, the value is between about 0.25 and about1.5%, in particular in the region of about 1%.

Organic solvents which can be used in the inventive pour-on solutions,mention may be made in particular of: acetyltributyl citrate, fatty acidesters such as the dimethyl ester, diisobutyl adipate, acetone,acetonitrile, benzyl alcohol, butyl diglycol, dimethylacetamide,dimethylformamide, dipropylene glycol n-butyl ether, ethanol,isopropanol, methanol, ethylene glycol monoethyl ether, ethylene glycolmonomethyl ether, monomethylacetamide, dipropylene glycol monomethylether, liquid polyoxyethylene glycols, propylene glycol, 2-pyrrolidone,in particular N-methylpyrrolidone, diethylene glycol monoethyl ether,ethylene glycol and diethyl phthalate, or a mixture of at least two ofthese solvents.

As vehicle or diluent for the inventive pour-on solutions, mention maybe made in particular of:

plant oils such as soybean oil, groundnut oil, castor oil, corn oil,cotton oil, olive oil, grape seed oil, sunflower oil, etc.; mineral oilssuch as petrolatum, paraffin, silicone, etc.; aliphatic or cyclichydrocarbons or alternatively, for example, medium-chain (C₈ to C₁₂ inparticular) triglycerides.

An emollient and/or spreading and/or film-forming agent will preferablybe added, this agent being selected in particular from:

polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetateand vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol,glycerol, sorbitol, polyoxyethylenated sorbitan esters; lecithin, sodiumcarboxymethylcellulose, silicone oils, polydiorganosiloxane oils, inparticular polydimethylsiloxane (PDMS) oils, for example thosecontaining silanol functionalities, or a 45V2 oil,

anionic surfactants such as alkaline stearates, in particular sodium,potassium or ammonium stearates; calcium stearate, triethanolaminestearate; sodium abietate; alkyl sulphates, in particular sodium laurylsulphate and sodium cetyl sulphate; sodium dodecylbenzenesulphonate,sodium dioctylsulphosuccinate; fatty acids, in particular those derivedfrom coconut oil,

cationic surfactants such as water-soluble quaternary ammonium salts offormula N⁺R′R″R′″R″″, Y⁻ in which the radicals R are optionallyhydroxylated hydrocarbon radicals and Y⁻ is an anion of a strong acidsuch as the halide, sulphate and sulphonate anions;cetyltrimethylammonium bromide is among the cationic surfactants whichcan be used,

amine salts of formula N⁺R′R″R′″ in which the radicals R are optionallyhydroxylated hydrocarbon radicals; octadecylamine hydrochloride is amongthe cationic surfactants which can be used,

nonionic surfactants such as sorbitan esters, which are optionallypolyoxyethylenated, in particular polysorbate 80, polyoxyethylenatedalkyl ethers; polyoxypropylated fatty alcohols such aspolyoxypropylene-styrol ether; polyethylene glycol stearate,polyoxyethylenated derivatives of castor oil, polyglycerol esters,polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids,copolymers of ethylene oxide and propylene oxide,

amphoteric surfactants such as the substituted lauryl compounds ofbetaine;

or a mixture of at least two of these agents.

The solvent will be used in proportion with the concentration of thecompound II and its solubility in this solvent.

The emollient is preferably used in a proportion of from about 0.1 toabout 10%, in particular from about 0.25 to about 5%, by volume.

This invention further provides for parasitical spray formulations whichcomprise:

a) an effective amount of an ectoparasitical combination comprising1-N-arylpyrazole derivative and amitraz; and

b) a pharmaceutical or veterinary acceptable liquid carrier vehicle.

Preferred carrier vehicles include isopropanol, ethanol, methanol,acetone, ether(s), propylene glycol, polyethylene glycol, glycol formal,DGME and DMSO.

EXAMPLES

The following non-limiting examples illustrate the invention:

Example 1

The following formulation according to the present invention wasprepared by conventional techniques:

Ingredient Amount (% w/v) fipronil 10.0 amitraz 5.0 ethanol 10.0polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02butylated hydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100

Example 2

The following formulation according to the present invention wasprepared by conventional techniques:

Ingredient Amount (% w/v) fipronil 10.0 amitraz 15.0 ethanol 10.0polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02butylated hydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100

Example 3

The following formulation according to the present invention wasprepared by conventional techniques:

Ingredient Amount (% w/v) fipronil 10.0 amitraz 12.0 ethanol 10.0polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02butylated hydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100

Comparative Example 4

The following formulation not according to the present invention wasprepared by conventional techniques:

Ingredient Amount (% w/v) fipronil 10.0 ethanol 10.0 polyvidone 5.0polysorbate 80 5.0 butylated hydroxyanisole 0.02 butylatedhydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100

Example 5

The duration of the efficacy of the formulation of Example 3 (accordingto the present invention) was compared with the formulation ofComparative Example 4 against ticks on dogs. The results are presentedbelow:

Duration of Efficacy against Rhipicephalus sanguineus ticks on dogs. (%efficacy at 48-hour counts) Days after Treatment 2 9 16 23 30 37 44 5158 Fipronil 10% 99.1% 100.0% 100.0% 100.0% 100.0%  87.6% 74.8% 66.2%36.3% Fipronil 10% + 99.1% 100.0% 100.0% 100.0% 100.0% 100.0% 94.8%84.1% 83.5% Amitraz 12%As can be seen the formulation according to the present inventionremained effective for a far longer period than fipronil alone.

Example 6

The speed of the efficacy of the formulation of Example 3 (according tothe present invention) was compared with the formulation of ComparativeExample 4 against ticks on dogs. The results are presented below:

Speed of efficacy against Rhipicephalus sanguineus ticks on dogs.(Efficacy counts were performed 6 hours after each weekly infestation)Days after Treatment 0 7 14 21 28 35 42 Fipronil 10% —  98.6%  91.0%21.3% 18.8%  7.9% — Fipronil 10% + Amitraz 12% 23.8% 100.0% 100.0% 95.6%95.2% 52.2% 7.6%As can be seen the formulation according to the present inventionexhibit a faster rate of efficacy than a formulation comprising fipronilalone.

Example 7

The duration of the efficacy of the formulation of Example 3 (accordingto the present invention) was compared with the formulation ofComparative Example 4 against fleas on dogs. The results are presentedbelow:

Duration of efficacy against fleas (% efficacy against fleas measured 24hours after each weekly infestation) Days after Treatment 2 23 30 37 4451 Fipronil 10% 100.0% 100.0%  99.0% 93.8% 69.4% 41.48% Fipronil 10% +100.0% 100.0% 100.0% 98.4% 96.3%  94.6% Amitraz 12%As can be seen the formulation according to the present inventionremained effective for a far longer period of time than a formulationcomprising fipronil alone. This enhanced efficacy is surprising sinceamitraz is not known in the art to be used in treating flea infestationson mammals and birds.

The above description is intended to be illustrative and not limiting.Various changes or modifications in the embodiments described herein mayoccur to those skilled in the art. These changes can be made withoutdeparting from the scope or spirit of the invention.

1. A veterinary parasitical spot-on formulation, which comprises: a) aveterinary parasiticidally effective amount of an ectoparasiticalcombination consisting essentially of fipronil and amitraz; and b) apharmaceutical or veterinary acceptable liquid carrier spot-onformulation vehicle for applying the formulation to a localized regionon an animal wherein the localized region is less than 10 cm² andwherein the formulation optionally includes a crystallization inhibitor.2. The parasitical spot-on formulation according to claim 1, wherein theliquid carrier vehicle comprises a solvent and a cosolvent wherein thesolvent is selected from the group consisting of acetone, acetonitrile,benzyl alcohol, butyl diglycol, dimethylacetamide, dimethylformamide,dipropylene glycol n-butyl ether, ethylene glycol monoethyl ether,ethylene glycol monomethyl ether, monomethylacetamide, dipropyleneglycol monomethyl ether, liquid polyoxyethylene glycols, propyleneglycol, 2-pyrrolidone, diethylene glycol monoethyl ether, ethyleneglycol, diethyl phthalate fatty acid esters, and a mixture of at leasttwo of these solvents and the cosolvent is selected from the groupconsisting of ethanol, isopropanol and methanol the crystallizationinhibitor selected from the group consisting of an anionic surfactant, acationic surfactant, a non-ionic surfactant, an amine salt, anamphoteric surfactant or polyvinylpyrrolidone, polyvinyl alcohols,copolymers of vinyl acetate and vinylpyrrolidone, polyethylene glycols,benzyl alcohol, mannitol, glycerol, sorbitol, polyoxyethylenatedsorbitan esters, lecithin, sodium carboxymethylcellulose, and acrylicderivatives, and a mixture of these crystallization inhibitors.
 3. Theparasitical spot-on composition according to claim 2, wherein theformulation further comprises an antioxidant.
 4. The parasitical spot-oncomposition according to claim 3, wherein the antioxidant is selectedfrom the group consisting of butylated hydroxyanisole, butylatedhydroxytoluene, ascorbic acid, sodium metabisulphite, propyl gallate andsodium thiosulphate.
 5. The parasitical spot-on formulation according toclaim 2, wherein water is present in a proportion of from 0 to about 30%v/v.
 6. The parasitical spot-on formulation according to claim 2,wherein the crystallization inhibitor is present in an amount from about1 to about 20% w/v.
 7. The parasitical spot-on formulation according toclaim 1 which comprises a crystallization inhibitor.
 8. The parasiticalspot-on formulation according to claim 2, wherein the anionic surfactantis alkaline stearates, sodium abietate; alkyl sulphates; sodiumdodecylbenzenesulphonate, sodium dioctylsulphosuccinate, and fattyacids; the cationic surfactant is water-soluble quaternary ammoniumsalts of formula N⁺R′R″R′″R″″Y⁻ in which the radicals R independentlyare hydrocarbon radicals, optionally hydroxylated, and Y⁻ is an anion ofa strong acid; the amine salt is an amine salt of N⁺R′R″R′″ in which theradicals R independently are optionally hydroxylated hydrocarbonradicals; the non-ionic surfactant is optionally polyoxyethylenatedsorbitan esters, polyoxyethylenated alkyl ethers, polyethylene glycolstearate, polyoxyethylenated derivatives of castor oil, polyglycerolesters, polyoxyethylenated fatty alcohols, polyoxyethylenated fattyacids, copolymers of ethylene oxide and propylene oxide; and theamphoteric surfactant is lauryl-substituted betaine compounds.
 9. Theparasitical spot-on formulation according to claim 3, wherein thecrystallization inhibitor is a crystallization inhibitor systemcomprising a polymeric film-forming agent and a surfactant.
 10. Theparasitical spot-on formulation according to claim 3, wherein thepolymeric film-forming agent is polyvinylpyrrolidone, polyvinylalcohols, or a copolymer of vinyl acetate and polyvinylpyrrolidone andthe surfactant is a non-ionic surfactant.
 11. The parasitical spot-onformulation according to claim 10, wherein the crystallization inhibitorsystem is a mixture of polyvinylpyrrolidone and polyoxethylene (20)sorbitan mono-oleate.
 12. The parasiticidal formulation of any one ofclaims 1-11, wherein the composition is prepared by mixing itsconstituents.
 13. The parasiticidal formulation of claim 12 wherein eachof the fipronil and amitraz is an active material, the vehicle includesa solvent as to each active material, and the mixing of the constituentsof the compositions comprises each active material being mixed in thesolvent as to each active material.
 14. The parasiticidal formulation ofclaim 13 wherein there are at least two solvents.
 15. The parasiticidalformulation of claim of claim 14 which includes an ester.
 16. Theparasiticidal formulation of claim 15 wherein the carrier includesisopropanol, ethanol, methanol, acetone, ether(s), propylene glycol,polyethylene glycol, glycol formal, di-ethylene glycol monomethyl ether(DGME), or dimethyl sulfoxide (DMSO).
 17. The parasiticidal formulationof claim 1 wherein the vehicle includes DMSO.
 18. The parasiticidalformulation of claim 1 wherein the vehicle includespolyvinylpyrrolidone.
 19. A parasitical spot-on formulation of claim 1,which comprises: a) an effective amount of an ectoparasiticalcombination consisting of fipronil and amitraz; b) wherein the carrierincludes di-ethylene glycol monomethyl ether and ethanol; and c)optionally, a crystallization inhibitor.